{{Rsnum
|rsid=1547201
|Chromosome=9
|position=96054202
|Orientation=plus
|GMAF=0.4894
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 23.1 | 46.2 | 30.8
| HCB | 18.2 | 34.1 | 47.7
| JPT | 13.6 | 63.6 | 22.7
| YRI | 22.2 | 50.8 | 27.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 18.2 | 34.1 | 47.7
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23382691
  |Trait=IgG glycosylation
  |Title=Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.
  |RiskAllele=C
  |Pval=4E-6
  |OR=.14
  |ORtxt=[0.083-0.206] unit decrease
  |OA=1
}}

{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}